Gene-specific Copy Number Variation Probe-FGF12
Add to Cart
| Catalog: |
CNVFP-FGF12-05216 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FGF12). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
FGF12 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FGF12 genes. This product achieves the purpose of detection by hybridizing with the FGF12 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Fibroblast Growth Factor 12 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. Two alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FGF12 |
| Location |
3q28-q29 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 191857181-192445388 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-FGF12-05216-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FGF12-05216-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FGF12-05216-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FGF12-05216-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FGF12-05216-AQ |
467nm |
418nm |
|
Other Products
